Gerstmann-Sträussler-Scheinker disease in an Alsatian family: clinical and genetic studies.
about
Transmissible and genetic prion diseases share a common pathway of neurodegeneration.Creutzfeldt-Jakob disease and the eye. I. Background and patient management.Inherited prion disease with an alanine to valine mutation at codon 117 in the prion protein gene.Genetic prion disease: Experience of a rapidly progressive dementia center in the United States and a review of the literature.Most pathogenic mutations do not alter the membrane topology of the prion protein.Combinatorial Control of Prion Protein Biogenesis by the Signal Sequence and Transmembrane Domain
P2860
Gerstmann-Sträussler-Scheinker disease in an Alsatian family: clinical and genetic studies.
description
1992 nî lūn-bûn
@nan
1992 թուականի Մարտին հրատարակուած գիտական յօդուած
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1992 թվականի մարտին հրատարակված գիտական հոդված
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1992年の論文
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1992年学术文章
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1992年学术文章
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1992年学术文章
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1992年学术文章
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1992年学术文章
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1992年學術文章
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name
Gerstmann-Sträussler-Scheinker ...... clinical and genetic studies.
@ast
Gerstmann-Sträussler-Scheinker ...... clinical and genetic studies.
@en
type
label
Gerstmann-Sträussler-Scheinker ...... clinical and genetic studies.
@ast
Gerstmann-Sträussler-Scheinker ...... clinical and genetic studies.
@en
prefLabel
Gerstmann-Sträussler-Scheinker ...... clinical and genetic studies.
@ast
Gerstmann-Sträussler-Scheinker ...... clinical and genetic studies.
@en
P2093
P2860
P356
P1476
Gerstmann-Sträussler-Scheinker ...... clinical and genetic studies.
@en
P2093
Chevalier Y
Kitamoto T
Steinmetz G
Tateishi J
Tranchant C
P2860
P304
P356
10.1136/JNNP.55.3.185
P407
P577
1992-03-01T00:00:00Z